MXPA03010142A - Novel arylheteroalkylamine derivatives. - Google Patents
Novel arylheteroalkylamine derivatives.Info
- Publication number
- MXPA03010142A MXPA03010142A MXPA03010142A MXPA03010142A MXPA03010142A MX PA03010142 A MXPA03010142 A MX PA03010142A MX PA03010142 A MXPA03010142 A MX PA03010142A MX PA03010142 A MXPA03010142 A MX PA03010142A MX PA03010142 A MXPA03010142 A MX PA03010142A
- Authority
- MX
- Mexico
- Prior art keywords
- arylheteroalkylamine
- derivatives
- novel
- compounds
- racemates
- Prior art date
Links
- 150000001875 compounds Chemical class 0.000 abstract 2
- HBAQYPYDRFILMT-UHFFFAOYSA-N 8-[3-(1-cyclopropylpyrazol-4-yl)-1H-pyrazolo[4,3-d]pyrimidin-5-yl]-3-methyl-3,8-diazabicyclo[3.2.1]octan-2-one Chemical class C1(CC1)N1N=CC(=C1)C1=NNC2=C1N=C(N=C2)N1C2C(N(CC1CC2)C)=O HBAQYPYDRFILMT-UHFFFAOYSA-N 0.000 abstract 1
- 206010065390 Inflammatory pain Diseases 0.000 abstract 1
- 102000008299 Nitric Oxide Synthase Human genes 0.000 abstract 1
- 108010021487 Nitric Oxide Synthase Proteins 0.000 abstract 1
- 208000027866 inflammatory disease Diseases 0.000 abstract 1
- 239000003112 inhibitor Substances 0.000 abstract 1
- 238000000034 method Methods 0.000 abstract 1
- 239000000203 mixture Substances 0.000 abstract 1
- 238000011321 prophylaxis Methods 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 238000002560 therapeutic procedure Methods 0.000 abstract 1
- 238000011282 treatment Methods 0.000 abstract 1
Classifications
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- C07D—HETEROCYCLIC COMPOUNDS
- C07D275/00—Heterocyclic compounds containing 1,2-thiazole or hydrogenated 1,2-thiazole rings
- C07D275/02—Heterocyclic compounds containing 1,2-thiazole or hydrogenated 1,2-thiazole rings not condensed with other rings
- C07D275/03—Heterocyclic compounds containing 1,2-thiazole or hydrogenated 1,2-thiazole rings not condensed with other rings with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
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- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D213/62—Oxygen or sulfur atoms
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Abstract
There are provided novel compounds of formula (I) wherein R1, R2, R3, R4, R5, R6, T, U, X, Y, V and W are as defined in the specification, and pharmaceutically acceptable salts thereof, and enantiomers and racemates thereof; together with processes for their preparation, compositions containing them and their use in therapy. The compounds are inhibitors of nitric oxide synthase and are thereby particularly useful in the treatment or prophylaxis of inflammatory disease and pain.
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
SE0101617A SE0101617D0 (en) | 2001-05-08 | 2001-05-08 | Novel compounds |
SE0103271A SE0103271D0 (en) | 2001-09-28 | 2001-09-28 | Novel compounds |
PCT/SE2002/000876 WO2002090332A2 (en) | 2001-05-08 | 2002-05-06 | Novel aeylheteroalkylaminε derivatives |
Publications (1)
Publication Number | Publication Date |
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MXPA03010142A true MXPA03010142A (en) | 2004-03-10 |
Family
ID=26655458
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
MXPA03010142A MXPA03010142A (en) | 2001-05-08 | 2002-05-06 | Novel arylheteroalkylamine derivatives. |
Country Status (15)
Country | Link |
---|---|
US (1) | US20040242871A1 (en) |
EP (1) | EP1572655A2 (en) |
JP (1) | JP2005506308A (en) |
KR (1) | KR20030096361A (en) |
CN (1) | CN100340548C (en) |
AR (1) | AR035700A1 (en) |
AU (1) | AU2002306039B2 (en) |
BR (1) | BR0209518A (en) |
CA (1) | CA2446120A1 (en) |
IL (1) | IL158388A0 (en) |
MX (1) | MXPA03010142A (en) |
NO (1) | NO20034970D0 (en) |
NZ (1) | NZ529107A (en) |
TW (1) | TWI278450B (en) |
WO (1) | WO2002090332A2 (en) |
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GB0004152D0 (en) | 2000-02-23 | 2000-04-12 | Astrazeneca Uk Ltd | Novel compounds |
SE0102640D0 (en) | 2001-07-31 | 2001-07-31 | Astrazeneca Ab | Novel compounds |
SE0203304D0 (en) * | 2002-11-07 | 2002-11-07 | Astrazeneca Ab | Novel Coumpounds |
WO2005080320A1 (en) | 2004-02-13 | 2005-09-01 | Warner-Lambert Company Llc | Androgen receptor modulators |
BRPI0509759A (en) | 2004-04-13 | 2007-10-16 | Warner Lambert Co | androgen modulators |
BRPI0509980A (en) | 2004-04-22 | 2007-10-16 | Warner Lambert Co | androgen modulators |
WO2006006065A1 (en) | 2004-07-08 | 2006-01-19 | Warner-Lambert Company Llc | Androgen modulators |
TW200724139A (en) | 2005-05-05 | 2007-07-01 | Warner Lambert Co | Androgen modulators |
US8183266B2 (en) * | 2007-06-04 | 2012-05-22 | Intra-Cellular Therapies, Inc. | Methods |
AU2008313660B2 (en) | 2007-10-19 | 2013-11-07 | Boehringer Ingelheim International Gmbh | Substituted piperidino-dihydrothienopyrimidines |
CN102256963B (en) | 2008-12-19 | 2014-06-11 | 贝林格尔.英格海姆国际有限公司 | Cyclic pyrimidin-4-carboxamides as ccr2 receptor antagonists for treatment of inflammation, asthma and copd |
PT3091012T (en) | 2009-12-17 | 2018-06-27 | Centrexion Therapeutics Corp | CCR2 RECEPTOR ANTAGONISTS AND THEIR USES |
WO2011073155A1 (en) | 2009-12-17 | 2011-06-23 | Boehringer Ingelheim International Gmbh | Novel antagonists for ccr2 and uses thereof |
EA201201052A1 (en) | 2010-01-29 | 2013-02-28 | Бёрингер Ингельхайм Интернациональ Гмбх | SUBSTITUTED NAFTYRIDINE AND THEIR APPLICATION AS KINASE SYK INHIBITORS |
WO2011141477A1 (en) | 2010-05-12 | 2011-11-17 | Boehringer Ingelheim International Gmbh | New ccr2 receptor antagonists, method for producing the same, and use thereof as medicaments |
US8877745B2 (en) | 2010-05-12 | 2014-11-04 | Boehringer Ingelheim International Gmbh | CCR2 receptor antagonists, method for producing the same, and use thereof as medicaments |
US8841313B2 (en) | 2010-05-17 | 2014-09-23 | Boehringer Ingelheim International Gmbh | CCR2 antagonists and uses thereof |
JP5636094B2 (en) | 2010-05-25 | 2014-12-03 | ベーリンガー インゲルハイム インターナショナル ゲゼルシャフト ミット ベシュレンクテル ハフツング | CCR2 receptor antagonist |
WO2011151251A1 (en) | 2010-06-01 | 2011-12-08 | Boehringer Ingelheim International Gmbh | New ccr2 antagonists |
WO2012101013A1 (en) | 2011-01-28 | 2012-08-02 | Boehringer Ingelheim International Gmbh | Substituted pyridinyl-pyrimidines and their use as medicaments |
EP2721025B1 (en) | 2011-06-16 | 2015-11-25 | Boehringer Ingelheim International Gmbh | New selective ccr2 antagonists |
JP5786258B2 (en) | 2011-07-15 | 2015-09-30 | ベーリンガー インゲルハイム インターナショナル ゲゼルシャフト ミット ベシュレンクテル ハフツング | Novel and selective CCR2 antagonist |
KR101986484B1 (en) | 2011-07-26 | 2019-06-10 | 베링거 인겔하임 인터내셔날 게엠베하 | Substituted quinolines and their use as medicaments |
US20130059866A1 (en) | 2011-08-24 | 2013-03-07 | Boehringer Ingelheim International Gmbh | Novel piperidino-dihydrothienopyrimidine sulfoxides and their use for treating copd and asthma |
US9096579B2 (en) | 2012-04-20 | 2015-08-04 | Boehringer Ingelheim International Gmbh | Amino-indolyl-substituted imidazolyl-pyrimidines and their use as medicaments |
WO2015140055A1 (en) | 2014-03-19 | 2015-09-24 | Boehringer Ingelheim International Gmbh | Heteroaryl syk inhibitors |
CN109096276B (en) * | 2018-08-01 | 2021-05-28 | 上海博志研新药物技术有限公司 | Preparation method of moxifloxacin hydrochloride and intermediate thereof |
CN112898285B (en) * | 2020-01-14 | 2022-05-24 | 河南师范大学 | Trifluoromethyl-containing bisoxazole compound, and synthesis method and application thereof in anti-cancer drugs |
CN115677572B (en) * | 2021-07-29 | 2024-05-28 | 武汉思瓴生物科技有限公司 | Fluoroamide derivative, pharmaceutical composition and application thereof |
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US2688638A (en) * | 1951-07-17 | 1954-09-07 | Givaudan Corp | Nu-(beta-phenoxyethyl) haloethylamines |
US4314081A (en) * | 1974-01-10 | 1982-02-02 | Eli Lilly And Company | Arloxyphenylpropylamines |
FR2432500A1 (en) * | 1978-02-24 | 1980-02-29 | Roussel Uclaf | NOVEL BENZENE PROPANAMINE DERIVATIVES AND SALTS THEREOF, PROCESS FOR THEIR PREPARATION AND APPLICATION AS MEDICAMENTS |
DE3138550A1 (en) * | 1981-09-28 | 1983-04-07 | Boehringer Ingelheim KG, 6507 Ingelheim | SUBSTITUTED 2-PHENYL-2- (PYRIDYLOXY) ETHYLAMINE AND ISOSTERIAL COMPOUNDS, METHOD FOR THE PRODUCTION AND USE THEREOF |
US4902710A (en) * | 1988-12-14 | 1990-02-20 | Eli Lilly And Company | Serotonin and norepinephrine uptake inhibitors |
SE9703693D0 (en) * | 1997-10-10 | 1997-10-10 | Astra Pharma Prod | Novel combination |
SE9803773D0 (en) * | 1998-11-05 | 1998-11-05 | Astra Pharma Prod | Compounds |
GB0004149D0 (en) * | 2000-02-23 | 2000-04-12 | Astrazeneca Uk Ltd | Novel compounds |
GB0004153D0 (en) * | 2000-02-23 | 2000-04-12 | Astrazeneca Uk Ltd | Novel use |
GB0004151D0 (en) * | 2000-02-23 | 2000-04-12 | Astrazeneca Uk Ltd | Novel use |
GB0004152D0 (en) * | 2000-02-23 | 2000-04-12 | Astrazeneca Uk Ltd | Novel compounds |
DK1453844T3 (en) * | 2001-11-21 | 2014-02-10 | Univ Aarhus | APPLICATION OF GLYCOSIDES OF MONO- AND DIACYLGYLCEROL AS ANTI-INFLAMMATORY AGENTS |
SE0203304D0 (en) * | 2002-11-07 | 2002-11-07 | Astrazeneca Ab | Novel Coumpounds |
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2002
- 2002-04-30 AR ARP020101589A patent/AR035700A1/en not_active Application Discontinuation
- 2002-05-06 BR BR0209518-1A patent/BR0209518A/en not_active IP Right Cessation
- 2002-05-06 EP EP02733658A patent/EP1572655A2/en not_active Withdrawn
- 2002-05-06 TW TW091109347A patent/TWI278450B/en not_active IP Right Cessation
- 2002-05-06 WO PCT/SE2002/000876 patent/WO2002090332A2/en active Application Filing
- 2002-05-06 JP JP2002587412A patent/JP2005506308A/en active Pending
- 2002-05-06 AU AU2002306039A patent/AU2002306039B2/en not_active Expired - Fee Related
- 2002-05-06 NZ NZ529107A patent/NZ529107A/en unknown
- 2002-05-06 MX MXPA03010142A patent/MXPA03010142A/en not_active Application Discontinuation
- 2002-05-06 CN CNB028096185A patent/CN100340548C/en not_active Expired - Fee Related
- 2002-05-06 KR KR10-2003-7014492A patent/KR20030096361A/en not_active Ceased
- 2002-05-06 US US10/476,958 patent/US20040242871A1/en not_active Abandoned
- 2002-05-06 IL IL15838802A patent/IL158388A0/en unknown
- 2002-05-06 CA CA002446120A patent/CA2446120A1/en not_active Abandoned
-
2003
- 2003-11-07 NO NO20034970A patent/NO20034970D0/en not_active Application Discontinuation
Also Published As
Publication number | Publication date |
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JP2005506308A (en) | 2005-03-03 |
AR035700A1 (en) | 2004-06-23 |
CN1630637A (en) | 2005-06-22 |
NZ529107A (en) | 2006-10-27 |
EP1572655A2 (en) | 2005-09-14 |
US20040242871A1 (en) | 2004-12-02 |
TWI278450B (en) | 2007-04-11 |
CN100340548C (en) | 2007-10-03 |
WO2002090332A2 (en) | 2002-11-14 |
AU2002306039B2 (en) | 2008-05-29 |
BR0209518A (en) | 2004-07-13 |
KR20030096361A (en) | 2003-12-24 |
CA2446120A1 (en) | 2002-11-14 |
NO20034970D0 (en) | 2003-11-07 |
WO2002090332A3 (en) | 2007-11-01 |
IL158388A0 (en) | 2004-05-12 |
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